NDC 50090-6218

SEGLUROMET

Ertugliflozin And Metformin Hydrochloride

SEGLUROMET is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Ertugliflozin Pidolate; Metformin Hydrochloride.

• Product ID: 50090-6218_63ca4364-3620-402e-accc-1c231ac85173
• NDC: 50090-6218
• Product Type: Human Prescription Drug
• Proprietary Name: SEGLUROMET
• Generic Name: Ertugliflozin And Metformin Hydrochloride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-12-19
• Marketing Category: NDA /
• Application Number: NDA209806
• Labeler Name: A-S Medication Solutions
• Substance Name: ERTUGLIFLOZIN PIDOLATE; METFORMIN HYDROCHLORIDE
• Active Ingredient Strength: 3 mg/1; mg/1
• Pharm Classes: Biguanide [EPC], Biguanides [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 50090-6218-0

60 TABLET, FILM COATED in 1 BOTTLE (50090-6218-0)

• Marketing Start Date: 2022-11-10
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "SEGLUROMET" or generic name "Ertugliflozin And Metformin Hydrochloride"

NDC	Brand Name	Generic Name
0006-5369	SEGLUROMET	ertugliflozin and metformin hydrochloride
0006-5370	SEGLUROMET	ertugliflozin and metformin hydrochloride
0006-5373	SEGLUROMET	ertugliflozin and metformin hydrochloride
0006-5374	SEGLUROMET	ertugliflozin and metformin hydrochloride
50090-6217	SEGLUROMET	ertugliflozin and metformin hydrochloride
50090-6218	SEGLUROMET	ertugliflozin and metformin hydrochloride
50090-6231	SEGLUROMET	ertugliflozin and metformin hydrochloride